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Variant (rsID / SNP)

rs78657998

DHX34

rs78657998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHX34. Location: chromosome 19, position 47,883,096. The table records no clinical significance for this variant.

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Reference-table entries

DHX34Not classified
Variant type
missense_variant
Chromosome / position
19:47883096
HGVS
NM_014681.6,c.2836C>T,p.Leu946Phe
Allele change
Missense_L946F

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.